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“Henke-Sass Wolf” Sinuscopes - Taiwan Registration 039173d7b2f9cb1ea4ed2aa2c6032b68

Access comprehensive regulatory information for “Henke-Sass Wolf” Sinuscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 039173d7b2f9cb1ea4ed2aa2c6032b68 and manufactured by HENKE-SASS, WOLF GMBH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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039173d7b2f9cb1ea4ed2aa2c6032b68
Registration Details
Taiwan FDA Registration: 039173d7b2f9cb1ea4ed2aa2c6032b68
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Device Details

“Henke-Sass Wolf” Sinuscopes
TW: “漢克薩斯沃夫”鼻竇鏡
Risk Class 2
MD

Registration Details

039173d7b2f9cb1ea4ed2aa2c6032b68

Ministry of Health Medical Device Import No. 031392

DHA05603139206

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT device

G4760 Nasopharyngeal scope (soft or rigid) and its accessories

Imported from abroad

Dates and Status

Aug 08, 2018

Aug 08, 2028